Petersen K R, Skouby S O, Sidelmann J, Jespersen J
Diabeteslaboratoriet og føde- og gynaekologisk afdeling Y, Rigshospitalet, København.
Ugeskr Laeger. 1994 Jan 10;156(2):187-90.
Thirty-four healthy young women were allocated to 12 consecutive cycles of treatment with monophasic combinations of: 20 micrograms ethinyl estradiol and 150 micrograms desogestrel (n = 15) or 30 micrograms ethinyl estradiol and 75 micrograms gestodene (n = 19). In both groups plasma levels of fibrinogen and factor VII increased while the capacity of coagulation inhibition was affected by increased protein C and decreased protein S levels. Increased fibrinolytic capacity was indicated by elevated activity and reduced antigen levels of tissue plasminogen activator and reduced activity and concentration of tissue plasminogen activator inhibitor. The ratio between thrombin-antithrombin-III-complexes and fibrin degradation products were unchanged signifying no effect of hormonal intake on the balance between thrombin formation and fibrin resolution. In conclusion, the dynamic balance between generation and resolution of fibrin was undisturbed during treatment with both hormonal compounds and our findings do not provide evidence for increased risk of thrombosis in normal women.
34名健康年轻女性被分配接受连续12个周期的单相联合治疗,治疗药物分别为:20微克炔雌醇和150微克去氧孕烯(n = 15)或30微克炔雌醇和75微克孕二烯酮(n = 19)。两组中,纤维蛋白原和凝血因子VII的血浆水平均升高,而凝血抑制能力受到蛋白C水平升高和蛋白S水平降低的影响。纤溶能力增强表现为组织纤溶酶原激活物活性升高、抗原水平降低,以及组织纤溶酶原激活物抑制剂活性和浓度降低。凝血酶 - 抗凝血酶 - III复合物与纤维蛋白降解产物之间的比率未发生变化,这表明激素摄入对凝血酶形成和纤维蛋白溶解之间的平衡没有影响。总之,在使用这两种激素化合物治疗期间,纤维蛋白生成与溶解之间的动态平衡未受干扰,我们的研究结果并未提供正常女性血栓形成风险增加的证据。